Evidence map›Paper›PMID 26925837›Full record

ArticlePLoS genetics2016

Genomics of Rapid Incipient Speciation in Sympatric Threespine Stickleback.

David A Marques, Kay Lucek, Joana I Meier, Salome Mwaiko, Catherine E Wagner, Laurent Excoffier, Ole Seehausen

Abstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

83 citing papers in PubMed.

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  11. Genetics and the Evolution of Prezygotic Isolation.Cold Spring Harbor perspectives in biology · 2024
    Review
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  17. Maintenance of local adaptation despite gene flow in a coastal songbird.Evolution; international journal of organic evolution · 2022
    Article
  18. Genomic changes underlying repeated niche shifts in an adaptive radiation.Evolution; international journal of organic evolution · 2022
    Article
  19. Article
  20. Article

23 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

David A MarquesAquatic Ecology and Evolution, Institute of Ecology and Evolution, University of Bern, Bern, Switzerland.
Kay LucekAquatic Ecology and Evolution, Institute of Ecology and Evolution, University of Bern, Bern, Switzerland.
Joana I MeierAquatic Ecology and Evolution, Institute of Ecology and Evolution, University of Bern, Bern, Switzerland.
Salome MwaikoAquatic Ecology and Evolution, Institute of Ecology and Evolution, University of Bern, Bern, Switzerland.
Catherine E WagnerAquatic Ecology and Evolution, Institute of Ecology and Evolution, University of Bern, Bern, Switzerland.
Laurent ExcoffierComputational and Molecular Population Genetics Lab, Institute of Ecology and Evolution, University of Bern, Bern, Switzerland.
Ole SeehausenAquatic Ecology and Evolution, Institute of Ecology and Evolution, University of Bern, Bern, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ecological speciation is the process by which reproductively isolated populations emerge as a consequence of divergent natural or ecologically-mediated sexual selection. Most genomic studies of ecological speciation have investigated allopatric populations, making it difficult to infer reproductive isolation. The few studies on sympatric ecotypes have focused on advanced stages of the speciation process after thousands of generations of divergence. As a consequence, we still do not know what genomic signatures of the early onset of ecological speciation look like. Here, we examined genomic differentiation among migratory lake and resident stream ecotypes of threespine stickleback reproducing in sympatry in one stream, and in parapatry in another stream. Importantly, these ecotypes started diverging less than 150 years ago. We obtained 34,756 SNPs with restriction-site associated DNA sequencing and identified genomic islands of differentiation using a Hidden Markov Model approach. Consistent with incipient ecological speciation, we found significant genomic differentiation between ecotypes both in sympatry and parapatry. Of 19 islands of differentiation resisting gene flow in sympatry, all were also differentiated in parapatry and were thus likely driven by divergent selection among habitats. These islands clustered in quantitative trait loci controlling divergent traits among the ecotypes, many of them concentrated in one region with low to intermediate recombination. Our findings suggest that adaptive genomic differentiation at many genetic loci can arise and persist in sympatry at the very early stage of ecotype divergence, and that the genomic architecture of adaptation may facilitate this.

Indexed as

Genetic SpeciationSympatryAnimalsEcotypeGene FlowGene FrequencyGenetics, PopulationGenomeIslandsLakesPolymorphism, Single NucleotideQuantitative Trait LociRiversSelection, GeneticSmegmamorphaSwitzerland

Identifiers

PMID26925837
PMCPMC4771382

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.